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Hilbro

by HILBRO International (Pvt) Ltd. 1,000+ variants

Ref 14.0371.26

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-G278140371260C Basic UDI-DI G278140371260CUDI-DIDate21 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Toennis Vessel Splanchnectomy Fcps cvd 26cm
Model / Reference
14.0371.26
Primary DI / UDI-DI
G278140371260C
Basic UDI-DI
B-G278140371260C
EMDN Code
L03130401 Tissue and organ grasping forceps, reusable
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
PK-MF-000025041
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Hilbro International (Pvt) Limited

See all devices from Hilbro International (Pvt) Limited →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No